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Efficacy of Telemonitoring on CPAP Treatment Compliance in Obstructive Sleep Apnea (OSA) Patients

Efficacy of Telemonitoring on CPAP Treatment Compliance in Obstructive Sleep Apnea (OSA) Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02517346
Enrollment
100
Registered
2015-08-07
Start date
2015-01-31
Completion date
2015-12-31
Last updated
2016-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sleep Apnea Syndrome

Keywords

CPAP compliance, Telemonitoring, Standard management, Cost effectiveness

Brief summary

The purpose of this study is to compare the effectiveness of telemonitoring versus standard follow-up on CPAP treatment compliance in Obstructive Sleep Apnea Syndrome (OSAS).

Detailed description

Obstructive Sleep Apnea (OSA) is defined by the presence of repetitive episodes of upper airways collapse during sleep, leading to nocturnal hypoxemia, sleep fragmentation and daytime sleepiness. When untreated, OSA is a risk factor for arterial hypertension , cardiovascular and cerebrovascular diseases, road accidents and a worse quality of life. The application of a continuous positive airways pressure (CPAP) represents the first line therapy in patients with moderate to severe OSA. CPAP treatment improves daytime sleepiness and oxygen saturation , reduces cardiovascular risk, ameliorates neurobehavioral performance, improves quality of life and reduces road accidents. Despite its demonstrated efficacy, CPAP effectiveness is significantly limited by poor adherence. A closer follow up could improve CPAP adherence but it would take up more work and additional costs for sleep units. So on that account, the investigators propose a study to demonstrate that automatic home treatment monitoring of patients with OSA is a cost-effectiveness alternative approach to patient's management. Moreover, the investigators believe that telemonitoring could improve CPAP compliance and patient's satisfaction and reduce follow-up costs. Methods: Prospective and randomized study during three months. Patients diagnosed as OSA in St. Maria's Hospital (Sleep Unit) and requiring CPAP treatment, will be randomized into two groups differing in CPAP compliance monitoring and management . Group 1 Standard care Patients will be fitted with a mask and given a CPAP and instructed on how to use the device. Patients will follow the standard treatment management. All patients will be visited at 1 month at sleep unit. Patients will be checked about progress and adherence to therapy and any problems with their machine. Information will be downloaded from their machines (CPAP adherence, applied CPAP pressure, mask leak, and residual respiratory events…). Group 2 Telemonitoring Patients will be fitted with a mask and given a CPAP. Each CPAP device will be provided with a modem sending daily compliance information (CPAP adherence, CPAP pressure, mask leak, and residual respiratory events) to a web database. Patients of both 2 groups will be finally visited at 3 months at sleep unit.

Interventions

OTHERStandard follow-up

Standard management according to Spanish Respiratory Society guidelines in Sleep Unit.

OTHERTelemonitoring

Follow up by telemonitoring system during 3 months

Sponsors

ResMed
CollaboratorINDUSTRY
Asociacio Lleidatana de Respiratori
CollaboratorUNKNOWN
Sociedad Española de Neumología y Cirugía Torácica
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Men and Women over 18 years old * Diagnosed as OSA and requiring CPAP treatment * Written informed consent form signed.

Exclusion criteria

* Patients with impaired lung function (overlap syndrome, obesity hypoventilation syndrome, and restrictive disorders) * Severe heart failure * Severe chronic pathology associated * Psychiatric disorder * Periodic leg movements * Pregnancy * Other dyssomnias or parasomnias * Patients already treated with CPAP

Design outcomes

Primary

MeasureTime frameDescription
CPAP adherence at 3 months3 monthsNumber of hours of use per day of CPAP according to the internal clock of the CPAP device

Secondary

MeasureTime frameDescription
Abandons at 3 months3 monthsNumber of patients lost at follow up at 3 months of CPAP therapy.
Patients' satisfaction at 3 months3 monthsPatients will be asked to grade their satisfaction with the follow up care provided by telemonitoring /sleep unit using a questionnaire and a visual analogue scale.
Cost effectiveness at 3 months3 monthsCosts in each group (CPAP carrying charge, number of visits and calls, number of hospital admissions) will be compared.
Change from baseline in quality of life at 3 months3 monthsEuroQOL health questionnaire and visual analogue scale will be used.
Fast detection of the non-adherent patient with telemonitoring3 monthsWe assume that telemonitoring could quickly detect non- adherent patients.
Change in blood pressure at 3 months3 months
Change in body mass index at 3 months3 months
Adverse events at 3 months3 months
Change from baseline in witnessed apneas at 3 months3 monthsPatients will be asked about the persistence of witnessed apneas
Change from baseline in nocturia at 3 months3 monthsPatients will be asked about the presence of nocturia.
Change from baseline in daytime sleepiness at 3 months3 monthsEpworth sleepiness scale will be used.
Changes in nocturnal gasping at 3 months3 monthsPatients will be asked about the persistence of nocturnal gasping
Changes in sleep fragmentation at 3 months3 monthsPatients will be asked about the persistence of sleep fragmentation/maintenance insomnia
Presence of symptoms of restlees leg syndrome at 3 months3 monthsPatients will be asked about the presence of symptoms of restless leg syndrome
Change from baseline in snoring at 3 months3 monthsPatients will be asked about the persistence of snoring

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026